A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635528



Internal ID6675641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101459474..101559743hg38UCSC Ensembl
chr14:101925811..102026080hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38100270
hg19100270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15108808
SamplesNA06984
Known GenesDIO3OS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635528
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer